OXAZEPAM
Generic: OXAZEPAM
TruPharmaManufacturer
ORALRoute
OXAZEPAMActive Substance
1987-08-10Original Approval
OXAZEPAM is FDA application ANDA071026, sponsored by TP ANDA HOLDINGS. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
TOXICITY TO VARIOUS AGENTS
2,858 reports
2
DRUG ABUSE
1,522 reports
3
FALL
1,520 reports
4
HYPOTENSION
1,402 reports
5
DRUG INTERACTION
1,178 reports
6
COMA
1,109 reports
7
SOMNOLENCE
997 reports
8
DEPRESSED LEVEL OF CONSCIOUSNESS
955 reports
9
PAIN
900 reports
10
CONSTIPATION
868 reports